Department of Radiotherapy, European Institute of Oncology, via Ripamonti 435, Milan, Italy.
Strahlenther Onkol. 2013 Jun;189(6):448-55. doi: 10.1007/s00066-013-0345-y. Epub 2013 Apr 21.
To evaluate the outcome of robotic CyberKnife (Accuray Inc. Sunnyvale, USA)-based stereotactic radiotherapy (CBK-SRT) for oligometastic cancer patients.
Between May 2007 and December 2009, 95 patients with a total of 118 lesions underwent CBK-SRT (median dose 24 Gy in 3 fractions).
adult patients with limited volume cancer; suitability for SRT but not for other local therapies. Primary diagnoses included breast, lung, head and neck, gastrointestinal and other malignancies. Prostate cancer patients were excluded. Concomitant systemic therapy was given in 40 % of cases and median follow-up was 12 months. Toxicity and tumor response were evaluated using the Radiation Therapy Oncology Group/European Organization for Research and Treatment of Cancer (RTOG/EORTC) Scale and Response Evaluation Criteria in Solid Tumors RECIST.
Toxicity was rare and observed mainly in patients with comorbidities or uncontrolled cancer. Out of 87 evaluable lesions, complete radiological response, partial response, stabilization and progressive disease were observed in 15 (17 %), 25 (29 %), 34 (39 %) and 13 (15 %) lesions, respectively. Upon restricting the analysis to lesions treated with CBK-SRT alone (no concomitant therapy), response- and local control (LC) rates remained similar. Actuarial 3-year in-field progression-free survival- (i.e. LC), progression-free survival- (PFS) and overall-survival (OS) rates were 67.6, 18.4, and 31.2 %, respectively. LC was reduced in cases of early recurrence. OS- and cause-specific survival (CSS) rates were significantly lower in patients treated for visceral lesions. Failures were predominantly out-field.
CBK-SRT is a feasible therapeutic approach for oligometastastic cancer patients that provides long-term in-field tumor control with a low toxicity profile. Further investigations should focus on dose escalation and optimization of the combination with systemic therapies.
评估立体定向放疗(CyberKnife,Accuray Inc.,美国)治疗寡转移癌患者的疗效。
2007 年 5 月至 2009 年 12 月,95 例患者共 118 个病灶接受了 CyberKnife 立体定向放疗(中位剂量 24Gy,3 次分割)。
局限性肿瘤成人患者;适合 SRT 治疗,但不适合其他局部治疗。主要诊断包括乳腺癌、肺癌、头颈部癌、胃肠道癌和其他恶性肿瘤。前列腺癌患者除外。40%的患者接受了同期全身治疗,中位随访时间为 12 个月。采用美国放射肿瘤学会(RTOG)/欧洲癌症研究与治疗组织(EORTC)毒性标准和实体瘤疗效评价标准(RECIST)评价毒性和肿瘤反应。
毒性罕见,主要见于合并症或未控制的癌症患者。87 个可评价病灶中,完全缓解、部分缓解、稳定和进展分别为 15 个(17%)、25 个(29%)、34 个(39%)和 13 个(15%)。仅分析单独接受 CyberKnife-SRT 治疗的病灶(无同期治疗),反应率和局部控制率相似。3 年局部无进展生存率(LC)、无进展生存率(PFS)和总生存率(OS)分别为 67.6%、18.4%和 31.2%。早期复发的 LC 降低。治疗内脏转移病灶的患者 OS 和疾病特异性生存率(CSS)明显降低。失败主要发生在野内。
CyberKnife 立体定向放疗是治疗寡转移癌患者的一种可行的治疗方法,具有长期的肿瘤控制效果,毒性较小。进一步的研究应集中在提高剂量和优化与全身治疗的联合治疗上。